Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K903326
›
Descendants
Devices descending from K903326
3 later devices reach Nidek US-2000 through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K020876
Echoscan, Model US-1800
Nidek, Inc.
2002
2
—
+2
K133132
Optical Biometer AL-Scan
Nidek Co., Ltd.
2014
0
1
+2
K042099
Tonopach Ultrasonic Tonometer/Pachymeter Model P-201 (the Tonopach)
Retinapharma Technologies, Inc.
2004
0
—